Clinical Trials Directory

Trials / Unknown

UnknownNCT02206789

Evaluation of the Efficacy of 2% Cyclosporine in Preventing Graft Rejection

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Aravind Eye Care System · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Aim/ Objective: Study consists of 2 separate and distinct entities A. Evaluation of the efficacy of 2% cyclosporine in preventing graft rejection in primary grafts w/o high risk characteristics study 1 (PKP study) B. Evaluation of the efficacy of 2% cyclosporine in preventing graft rejection in therapeutic keratoplasty- study 2(TKP study) Materials \& Methods: In both arms Patients requiring keratoplasty, above the age of 18 whom satisfactorily meet The inclusion criteria are different for each study Eligible candidates will be enrolled after signing an Informed Consent form Patients will be randomized into one of 2 groups * Only on topical steroids group A * On topical steroids + 2% cyclosporine Group B Study design: Prospective, randomized non-blinded study at a single centre. Methodology In both arms 1\. Schedule of topical steroid administration : 6 times for 2 weeks; 5 times for 2 weeks; 4 times for a month; 3 times for a month, and, subsequently twice-a-day until 1 year is completed Systemic steroids may be administered in the initial 2 weeks at the discretion of the investigators. (For all patients with fungal keratitis topical steroids can preferrably be administered only after 2 weeks post keratoplasty.) Until then voveran ophtha may be used 3\. Patients randomized to receive 2% cyclosporine will receive the same 3 times a day for 2years 4\. All patients will be followed for a minimum period of 2 years 5\. Follow up schedule - at 1 week, 2 weeks, 1 month, 2 months, 3 months, then every 3 months until 2 years are completed 6\. All episodes of graft rejection will be treated as per accepted norms and the patient will no longer follow the standardized protocol for steroid administration

Conditions

Interventions

TypeNameDescription
DRUGPrednisolone acetate1%,efficacy of prednisolone acetate1%alone versus prednisolone acetate 1%and cyclosporine 2% in preventing graft rejection
DRUGPrednisolone acetate1%, cyclosporine 2%penetrating keratoplasty--efficacy of prednisolone acetate1%alone versus prednisolone acetate 1%and cyclosporine 2% in preventing graft rejection

Timeline

Start date
2012-02-01
Primary completion
2017-02-01
Completion
2017-12-01
First posted
2014-08-01
Last updated
2014-08-01

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT02206789. Inclusion in this directory is not an endorsement.